BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INRATIO

    MDR report key: 2003816 · Received February 7, 2011

    Report

    Report Number
    2027969-2011-00263
    Event Type
    Malfunction
    Date Received
    February 7, 2011
    Date of Event
    November 15, 2010
    Report Date
    February 7, 2011
    Manufacturer
    ALERE SAN DIEGO, INC.
    Product Code
    GJS
    PMA / PMN Number
    021923
    Removal / Correction Number
    NI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION PENDING.

    Description of Event or Problem · 1

    CALLER REPORTED CORRELATION DATA BETWEEN INRATIO METER AND LAB FOR SEVERAL PTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INRATIO PROTHROMBIN TIME TEST GJS ALERE SAN DIEGO, INC. 100071 239277

    Patients

    Seq Age Sex Outcome Treatment
    1 NI